Canonical Allele Identifier: CA416047217

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17371375T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044880T>C , CM000663.2:g.17044880T>C	GRCh38
NC_000001.10:g.17371375T>C , CM000663.1:g.17371375T>C	GRCh37
NC_000001.9:g.17243962T>C	NCBI36
NG_012340.1:g.14291A>G , LRG_316:g.14291A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.-91A>G	ENSP00000481376.2:n.-91A>G
ENST00000491274.6:c.39A>G	ENSP00000480482.2:p.Arg13=
ENST00000375499.8:c.81A>G MANE Select	ENSP00000364649.3:p.Arg27=
ENST00000375499.7:c.81A>G	ENSP00000364649.3:p.Arg27=
ENST00000463045.2:c.-91A>G	ENSP00000481376.1:n.-91A>G
ENST00000466613.2:n.93A>G
ENST00000485515.5:n.69A>G
ENST00000491274.5:c.39A>G	ENSP00000480482.1:p.Arg13=
NM_003000.2:c.81A>G , LRG_316t1:c.81A>G	NP_002991.2:p.Arg27=
NM_003000.3:c.81A>G MANE Select	NP_002991.2:p.Arg27=